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Donor-specific toxicity of copanlisib identified using immune-humanized mice. [PDF]

open access: yesCancer Immunol Immunother
Becker RE   +4 more
europepmc   +1 more source
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Synthesis of quinazolinones and quinazolines

Tetrahedron, 2005
AbstractFor Abstract see ChemInform Abstract in Full Text.
Timothy P O'Sullivan   +2 more
exaly   +2 more sources

Pyrrolo[3,2-h]quinazolines as Photochemotherapeutic Agents

open access: yesChemMedChem, 2011
Heteroanalogues of angelicin, pyrrolo[3,2-h]quinazolines, were synthesized with the aim of obtaining new potent photochemotherapeutic agents. Many derivatives caused a significant decrease in cell proliferation in several human tumor cell lines after ...
Ignazio Castagliuolo   +2 more
exaly   +3 more sources

Quinazolines. Part XV. Hexahydro- and octahydro-quinazolines

Journal of the Chemical Society C: Organic, 1971
3,4,5,6,7,8-Hexahydroquinazoline, obtained by catalytic reduction of 5,6,7,8-tetrahydroquinazoline, was slowly oxidised by air to the starting material in chloroform solution, but in aqueous alkali it was degraded to 2-formamidomethylcyclohexanone. trans-4a,5,6,7,8,8a-Hexahydroquinazolin-4(1 - or 3-H)-one was shown to be a tautomeric mixture of the (1H)
W. L. F. Armarego, Toshihiko Kobayashi
openaire   +1 more source

Quinazolines

ChemInform, 2005
AbstractFor Abstract see ChemInform Abstract in Full Text.
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The Quinazoline Alkaloids

1984
Quinazoline (1) is a building block for approximately eighty naturally occurring alkaloids isolated from a number of families of the plant kingdom, from microorganisms and from animals. The first known quinazoline alkaloid was vasicine (peganine), isolated in 1888 from Adhatoda vasica, and later from other species.
openaire   +2 more sources

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Frontiers in Chemistry, 2021
Aamer Saeed
exaly  

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